U.S. flag

An official website of the United States government

GTR Home > Conditions/Phenotypes > Brachydactyly type E1

Brachydactyly type E1

Summary

Any brachydactyly type E in which the cause of the disease is a mutation in the HOXD13 gene. [from MONDO]

Available tests

22 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (22 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: BDE, BDSD, HOX4I, SPD, SPD1, HOXD13
    Summary: homeobox D13

Clinical features

Help
Imported from Human Phenotype Ontology (HPO)

Show allHide all

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.